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Atom bomb tests used to age our immune system

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Swedish scientists have used a radioactive isotope released by atomic bomb tests in the 1950s and 60s to test how our immune system ages. Carbon-14 isotopes released during the nuclear weapons tests have been incorporating into our DNA for decades, providing a unique opportunity to carbon date our immune-defending T cells. The researchers found our T cells constantly replicate, but the turnover slows down with age from an average of 1.7 years in 20–30-year-olds to 6.6 years in 50–65-year-olds. Since these cells may divide only once every 5-10 years in older adults, this may explain why we are able to maintain a stable population of T cells for decades after we can no longer produce new ones.

Journal/conference: PLOS Biology

Link to research (DOI): 10.1371/journal.pbio.3000383

Organisation/s: Karolinska Institute, Sweden

Funder: This research was funded by grants from the Swedish Research Council, Swedish Cancer Society, Strategic Research Programme in Stem Cells and Regenerative Medicine, Knut och Alice Wallenbergs Stiftelse, Torsten Soderbergs Stiftelse, Portuguese Foundation for Science and Technology, Human Frontiers Long-Term Fellowship and the Swedish Society for Medicine.

Media Release

From: PLOS

Old atom bomb tests help scientists see how the human immune system ages

T cells are in constant turnover, but regulatory systems maintain diversity

The pulse of environmental carbon-14 released by atom bomb tests in the early years of the Cold War has allowed researchers to understand how humans can still mount an immune response to diverse pathogens well into their 50’s and 60’s, according to a study led by Jonas Frisén at the Karolinska Institute in Sweden, publishing on October 29 in the open-access journal PLOS Biology.

T cells, which are produced by the thymus and represent one of the major arms of our immune defences, have unique and highly variable cell surface receptors that allow them to detect specific molecular patterns presented by pathogens or cancerous cells. Thus, the diversity of a person’s T cell repertoire determines the diversity of pathogens and cancer cells that their immune system can target. But as we age, new T cells are no longer produced by the thymus; instead the T cell pool is maintained by existing T cells replicating clonally.

To investigate how this process is regulated to prevent a loss of T cell diversity with age, the researchers isolated naïve T cells from blood samples of 59 healthy adults and exploited a unique global “experiment.” During the 1950s and 60s, the nuclear weapon tests resulted in a substantial global release into the atmosphere of the radioactive isotope carbon-14 that has since been incorporated into the DNA of the human population.

This handy pulse allowed the scientists to use carbon-14 DNA dating to probe the life history of T cell populations. They found that there is a constant turnover of all naïve T cells, but the frequency of cell turnover declines with age from an average of 1.7 years in 20-30-year-olds to 6.6 years in 50-65-year-olds, helping individuals to maintain T cell numbers despite the declining production in the thymus.

The authors also used mass cytometry to show that levels of the CD31 protein–which is highest in T cells produced by the thymus but then progressively dilutes with each clonal division–are correlated with phosphorylation of a transcription factor, NF-kB, which is known to be essential for T cell replication. This means that T cell clones that have divided many times since their production (and are therefore more numerous) are less likely to do so again. The authors suggest that this negative feedback loop may help to prevent certain T cell types coming to dominate the immune cell pool, which would thereby reduce the diversity of pathogens that can be detected.

“Naive T cells divide extremely slowly relative to other immune cells, which has made it difficult to study how the population behaves throughout a human lifetime. The fact that these cells may divide only once every 5-10 years in older adults provides a simple explanation for how we are able to maintain a stable population of naïve T cells for decades after new T cell production ceases. It will be interesting to next understand how this process works in very old individuals, as it is becoming increasingly clear that loss of naïve T cell numbers and clonal diversity may be associated with immune defects in persons over 70 years of age.” says Jeff Mold, first-author of the paper


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